A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112247



Internal ID21295513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:80159790..80163067hg38UCSC Ensembl
Innerchr11:79870834..79874111hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg383278
hg193278
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv213n145
Supporting Variantsnssv14091806, nssv14091126
Samplessample60, sample187
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112247
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer